The Science and Economics of Prevention

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Unknown venue

• Publication date

  Unknown publication date

• Fields of study

  Economics, Political Science

• Identifiers

  No identifiers available.

• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• A grand challenge: Providing benefits of clinical genetics to those in need

  2011cited by this paper
• Initial impact of the sequencing of the human genome

  2011cited by this paper
• Deflating the Genomic Bubble

  2011cited by this paper
• Charting a course for genomic medicine from base pairs to bedside

  2011cited by this paper
• Functional Variants in MBL2 Are Associated With Type 2 Diabetes and Pre-Diabetes Traits in Pima Indians and the Old Order Amish

  2010cited by this paper
• STRADalpha deficiency results in aberrant mTORC1 signaling during corticogenesis in humans and mice.

  2010cited by this paper
• Clinical assessment incorporating a personal genome.

  2010cited by this paper
• Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome.

  2010cited by this paper
• A de novo paradigm for mental retardation

  2010cited by this paper
• Only Connect

  2010cited by this paper
• Lack of replication of genetic predictors for the rheumatoid arthritis response to anti-TNF treatments: a prospective case-only study

  2010cited by this paper
• Concise Encyclopedia of Amish, Brethren, Hutterites, and Mennonites

  2010cited by this paper
• TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.

  2010cited by this paper
• Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.

  2010cited by this paper
• The molecular basis of autosomal recessive diseases among the Arabs and Druze in Israel

  2010cited by this paper
• Evaluation of A2BP1 as an Obesity Gene

  2010cited by this paper
• What is value in health care?

  2010cited by this paper
• Quantifying uncertainty in genotype calls

  2010cited by this paper
• Putting the value framework to work.

  2010cited by this paper
• Classical maple syrup urine disease and brain development: principles of management and formula design.

  2010cited by this paper
• Recommendations for Genetic Variation Data Capture in Developing Countries to Ensure a Comprehensive Worldwide Data Collection

  2010cited by this paper
• Exome sequencing reveals VCP mutations as a cause of familial ALS.

  2010cited by this paper
• Variability in GWAS analysis: the impact of genotype calling algorithm inconsistencies

  2010cited by this paper
• Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder

  2010cited by this paper
• Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma

  2010cited by this paper
• Altered Functional Connectivity in Frontal Lobe Circuits Is Associated with Variation in the Autism Risk Gene CNTNAP2

  2010cited by this paper
• Genome-wide association studies of coronary artery disease and heart failure: where are we going?

  2009cited by this paper
• Reconstructing Indian Population History

  2009cited by this paper
• Detecting new neurodegenerative disease genes: does phenotype accuracy limit the horizon?

  2009cited by this paper
• A framework for interpreting genome-wide association studies of psychiatric disorders

  2009cited by this paper
• From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

  2009cited by this paper
• The Disruptive Nature of Personalized Medicine Technologies: Implications for the Health Care System

  2009cited by this paper
• Genetics, medicine, and the Plain people.

  2009cited by this paper
• Contact in the genetics of autism and schizophrenia.

  2009cited by this paper
• Translating scientific opportunity into public health impact: a strategic plan for research on mental illness.

  2009cited by this paper
• From a declaration of values to the creation of value in global health: A report from Harvard University's Global Health Delivery Project

  2009cited by this paper
• CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila.

  2009cited by this paper
• Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

  2009cited by this paper
• A functional genetic link between distinct developmental language disorders.

  2008cited by this paper
• A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

  2008cited by this paper
• Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.

  2008cited by this paper
• Polymorphisms associated with cholesterol and risk of cardiovascular events.

  2008cited by this paper
• CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

  2008cited by this paper
• Living apart together: reflections on bioethics, global inequality and social justice

  2008cited by this paper
• The next steps for genomic medicine: challenges and opportunities for the developing world

  2008cited by this paper
• Expectations and challenges stemming from genome-wide association studies.

  2008cited by this paper
• Universal health care, genomic medicine and Thailand: investing in today and tomorrow

  2008cited by this paper
• Genome study of kidney disease in the age of post genome-sequencing.

  2008cited by this paper
• Genomic medicine and developing countries: creating a room of their own

  2008cited by this paper
• A Review of Public Policy Issues in Promoting the Development and Commercialization of Pharmacogenomic Applications: Challenges and Implications

  2008cited by this paper
• Clinical application of DNA microarrays: molecular diagnosis and HLA matching of an Amish child with severe combined immune deficiency.

  2008cited by this paper
• Genome-wide analyses of human perisylvian cerebral cortical patterning

  2007cited by this paper
• Genetic structure of circumpolar populations: A synthesis

  2007cited by this paper
• Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5.

  2007cited by this paper
• Use of array-based technology in the practice of medical genetics

  2007cited by this paper
• Prevention of brain disease from severe 5,10-methylenetetrahydrofolate reductase deficiency.

  2007cited by this paper
• Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation

  2006cited by this paper
• Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.

  2006cited by this paper
• US biomedical research: basic, translational, and clinical sciences.

  2005cited by this paper
• Population history and its impact on medical genetics in Quebec

  2005cited by this paper
• Genome‐wide SNP arrays as a diagnostic tool: Clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite population

  2005cited by this paper
• Translational and clinical science--time for a new vision.

  2005cited by this paper
• The burden of genetic disease on inpatient care in a children's hospital.

  2004cited by this paper
• The Commercialisation of Medical and Scientific Reporting

  2004cited by this paper
• Economic costs associated with mental retardation, cerebral palsy, hearing loss, and vision impairment--United States, 2003.

  2004cited by this paper
• Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function.

  2004cited by this paper
• Impact of molecular medicine on pathophysiology, medical practice, and medical education.

  2003cited by this paper
• Pediatric medicine and the genetic disorders of the Amish and Mennonite people of Pennsylvania

  2003cited by this paper
• Disseminating innovations in health care.

  2003cited by this paper
• DNA: The Secret of Life

  2003cited by this paper
• A vision for the future of genomics research

  2003cited by this paper
• Shattuck lecture--clinical research to clinical practice--lost in translation?

  2003cited by this paper
• Diagnosis and treatment of maple syrup disease: a study of 36 patients.

  2002cited by this paper
• Implications of the Human Genome Project for medical science.

  2001cited by this paper
• Metachromatic leukodystrophy in the Navajo: fallout of the American-Indian wars of the nineteenth century.

  2001cited by this paper
• The anatomy of the human genome: a neo-Vesalian basis for medicine in the 21st century.

  2001cited by this paper
• Genomic medicine: who will practice it? A call to open arms.

  2001cited by this paper
• Human population genetics: lessons from Finland.

  2001cited by this paper
• The world health report 2000 - Health systems: improving performance

  2000cited by this paper
• Breaking Down the Walls: Thoughts on the Scholarship of Integration

  2000cited by this paper
• Diagnostic yield of the comprehensive assessment of developmental delay/mental retardation in an institute of child neuropsychiatry.

  1999cited by this paper
• The clinical investigator: bewitched, bothered, and bewildered--but still beloved.

  1997cited by this paper
• Genetic variation in India.

  1996cited by this paper
• Genetic differentiation and population structure of some occupational caste groups in Uttar Pradesh, India.

  1996cited by this paper
• Complex segregation analyses of old order Amish families ascertained through bipolar I individuals.

  1995cited by this paper
• The secret of life.

  1995cited by this paper
• Through my window--remarks at the 125th year celebration of Children's Hospital of Boston.

  1994cited by this paper
• Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania.

  1991cited by this paper
• Art of the soluble

  1988cited by this paper
• Outcome of early and long-term management of classical maple syrup urine disease.

  1981cited by this paper
• The care of the patient.

  1968cited by this paper
• The Child Who Never Grew

  1950cited by this paper
• Performance of Common Genetic Variants in Breast-cancer Risk Models

  year unknowncited by this paper
• Scientific Books: Les Physiciens Hollandais et la Methode Experimental en France au XVIIIeme Siecle; An Introduction to the Study of Experimental Medicine

  year unknowncited by this paper

• No citing papers are available for this paper.